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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Safety of belatacept bridging immunosuppression in hepatitis c-positive liver transplant recipients with renal dysfunction
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Safety of belatacept bridging immunosuppression in hepatitis c-positive liver transplant recipients with renal dysfunction

机译:贝拉西普桥接免疫抑制在丙型肝炎阳性肝移植肾功能不全患者中的安全性

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BACKGROUND: Perioperative renal dysfunction in liver transplant recipients complicates maintenance immunosuppressive therapy, particularly in patients with hepatitis C. Calcineurin inhibitors exacerbate renal dysfunction and mammalian target-of-rapamycin inhibitors are generally avoided because of perceived perioperative risks. The authors' experience with seven liver transplant patients who received belatacept and mycophenolic acid maintenance immunosuppression is reported. METHODS: A retrospective review of adult liver transplant recipients with hepatitis C receiving belatacept was conducted under Institutional Review Board approval. All patients were Epstein-Barr virus IgG seropositive. The primary endpoint was patient and graft survival, with secondary endpoints including the incidence of acute rejection, degree of renal function recovery, and occurrence of major side effects. RESULTS: Between December 19, 2011 and January 25, 2013, seven liver transplant recipients with hepatitis C received belatacept immunosuppression in the perioperative period. The primary indication for belatacept was perioperative renal dysfunction. Belatacept was initiated between 2 and 90 days posttransplant and the duration of belatacept therapy ranged from 19 to 89 days. Patients were transitioned onto calcineurin inhibitor therapy when they reached chronic kidney disease stage 2 or better. Six-month patient and graft survival was 86%. There was one episode of graft rejection on belatacept therapy in a patient who had also had early rejection before initiation of belatacept. CONCLUSIONS: The results in this initial group of patients suggest that belatacept with mycophenolic acid may be a safe maintenance immunosuppression regimen in hepatitis C-positive liver transplant recipients with renal dysfunction, and that this regimen can serve as an effective bridge to calcineurin inhibitor therapy.
机译:背景:肝移植受者的围手术期肾功能不全使维持免疫抑制治疗变得复杂,尤其是在丙型肝炎患者中。钙调神经磷酸酶抑制剂会加剧肾功能不全,通常由于避免了围手术期的风险而避免使用哺乳动物雷帕霉素靶标抑制剂。作者报道了七名接受贝拉西普和霉酚酸维持免疫抑制治疗的肝移植患者的经验。方法:在机构审查委员会的批准下,对接受贝拉西普治疗的丙型肝炎成人肝移植受者进行了回顾性审查。所有患者均为爱泼斯坦-巴尔病毒IgG血清阳性。主要终点是患者和移植物的存活,次要终点包括急性排斥反应的发生率,肾功能恢复程度和主要副作用的发生。结果:在2011年12月19日至2013年1月25日之间,七名丙型肝炎肝移植受者在围手术期接受了belatacept免疫抑制。贝拉西普的主要适应症是围手术期肾功能不全。 Belatacept在移植后2至90天之间开始,belatacept治疗的持续时间为19至89天。当患者达到慢性肾脏疾病第2阶段或更好的阶段时,就转用钙调神经磷酸酶抑制剂治疗。六个月的患者和移植物存活率为86%。一名患者在belacept疗法之前发生了一次移植排斥反应,该患者在开始belatacept之前也有早期排斥反应。结论:这组初始患者的结果表明,贝拉西普与麦考酚酸可能是对肾功能不全的丙型肝炎阳性肝移植患者的一种安全的维持免疫抑制方案,并且该方案可以作为钙调神经磷酸酶抑制剂治疗的有效桥梁。

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